01 1Pfizer Ireland Pharmaceuticals Unlimited Company
02 1Upjohn Manufacturing Ireland Unlimited Company
01 2Pfizer Korea
01 2Axitinib
01 2U.S.A
Registrant Name : Pfizer Korea
Registration Date : 2012-08-06
Registration Number : Su189-15-ND
Manufacturer Name : Upjohn Manufacturing Ireland...
Manufacturer Address : Little Island Co. Cork, T45 F627, Ireland
Registrant Name : Pfizer Korea
Registration Date : 2018-02-08
Registration Number : Su87-23-ND
Manufacturer Name : Pfizer Ireland Pharmaceutica...
Manufacturer Address : Ringaskiddy API Plant, Ringaskiddy, Co. Cork, P43 X336, Ireland
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A AG-13736 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AG-13736, including repackagers and relabelers. The FDA regulates AG-13736 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AG-13736 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of AG-13736 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A AG-13736 supplier is an individual or a company that provides AG-13736 active pharmaceutical ingredient (API) or AG-13736 finished formulations upon request. The AG-13736 suppliers may include AG-13736 API manufacturers, exporters, distributors and traders.
click here to find a list of AG-13736 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AG-13736 Drug Master File in Korea (AG-13736 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AG-13736. The MFDS reviews the AG-13736 KDMF as part of the drug registration process and uses the information provided in the AG-13736 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AG-13736 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their AG-13736 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AG-13736 suppliers with KDMF on PharmaCompass.
